Generate depictions of molecules and reactions from
SMILES
or
SDF
.
CN1C=NC2=C1C(=O)N(C(=O)N2C)C caffeine [Cs+].[O-]C(=O)[O-].[Cs+] Cs2CO3 [Li+].[Al+3].[H-].[H-].[H-].[H-] LiAlH4 Cl[Pt@SP1](Cl)([NH3])[NH3] cis-platin O=[N+]([O-])[Co@]([NH3])([NH3])([NH3])([NH3])[N+]([O-])(=O) trans-[Co(NH3)4(NO2)2] Cl*.Cl*.c1ccccc1-c1ccccc1 |m:1:4.5.6.7.8.9,3:10.11.12.13.14.15| dichlorobiphenyl CCOCCOCCO |Sg:n:3,4,5::ht| PEGn *c1ccccc1 |$_AP1$| phenyl CC(C)[C@H](N*)C(*)=O |$;;;;;_AP1;;_AP2;$| valine monomer c1(:*:c2c(:*:c1*)C(N(N2)*)=O)* |$;Y;;;X;;R10;;;;Z;;R11$| US 2007/0129374 (I) C*.C*.C1=CC=CC=C1C=2C(C=CN3C2C=*C(=*3)C**)=O.C* |$;R2;;R3;;;;;;;;;;;;;;W;;A;;X;R4;;;R1$,m:0:5.4.9.8.7.6,2:7.6.5.4.9.8,24:4.9.8.7.6.5,Sg:n:20:m:ht| US 2007/0129372 (I) [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].CCCCc1ccc(CO[C@H]2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@@H]2O[C@H]3O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](O[C@H]4O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](O[C@H]5O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@@H]5OS(=O)(=O)[O-])[C@@H]4OS(=O)(=O)[O-])[C@@H]3OS(=O)(=O)[O-])cc1 CHEMBL590010 CCO.[CH3:1][C:2](=[O:3])[OH:4]>[H+]>CC[O:4][C:2](=[O:3])[CH3:1].O Ethyl esterification [1.7.3] [CH3:9][CH:8]([CH3:10])[c:7]1[cH:11][cH:12][cH:13][cH:14][cH:15]1.[CH2:3]([CH2:4][C:5](=[O:6])Cl)[CH2:2][Cl:1]>[Al+3].[Cl-].[Cl-].[Cl-].C(Cl)Cl>[CH3:9][CH:8]([CH3:10])[c:7]1[cH:11][cH:12][c:13]([cH:14][cH:15]1)[C:5](=[O:6])[CH2:4][CH2:3][CH2:2][Cl:1] |f:2.3.4.5| Friedel-Crafts acylation [3.10.1] ClC1=NC=2N(C(=C1)N(CC3=CC=CC=C3)CC4=CC=CC=C4)N=CC2C(OCC)=O>C1(=CC(=CC(=N1)C)N)N2C[C@H](CCC2)O.O1CCOCC1.CC1(C2=C(C(=CC=C2)P(C3=CC=CC=C3)C4=CC=CC=C4)OC5=C(C=CC=C15)P(C6=CC=CC=C6)C7=CC=CC=C7)C.C=1C=CC(=CC1)\C=C\C(=O)\C=C\C2=CC=CC=C2.C=1C=CC(=CC1)\C=C\C(=O)\C=C\C2=CC=CC=C2.C=1C=CC(=CC1)\C=C\C(=O)\C=C\C2=CC=CC=C2.[Pd].[Pd].[Cs]OC(=O)O[Cs]>C1(=CC(=CC(=N1)C)NC2=NC=3N(C(=C2)N(CC4=CC=CC=C4)CC5=CC=CC=C5)N=CC3C(OCC)=O)N6C[C@H](CCC6)O>CO.C1CCOC1.O.O[Li]>C1(=CC(=CC(=N1)C)NC2=NC=3N(C(=C2)N(CC4=CC=CC=C4)CC5=CC=CC=C5)N=CC3C(O)=O)N6C[C@H](CCC6)O>CN(C)C(=[N+](C)C)ON1C2=C(C=CC=N2)N=N1.F[P-](F)(F)(F)(F)F.[NH4+].[Cl-].CN(C)C=O.CCN(C(C)C)C(C)C>C1(=CC(=CC(=N1)C)NC2=NC=3N(C(=C2)N(CC4=CC=CC=C4)CC5=CC=CC=C5)N=CC3C(N)=O)N6C[C@H](CCC6)O>>C1(=CC(=CC(=N1)C)NC2=NC=3N(C(=C2)N)N=CC3C(N)=O)N4C[C@H](CCC4)O |f:4.5.6.7.8,16.17,18.19| US20190241576A1
Color on White
Color on Black
Color on Clear
Black on White
Black on Clear
White on Black
Neon on Black
No Annotation
Atom Numbers
Atom Mapping
Color Map
Atom Value
CIP Stereo Label
Minimal Hydrogens
Input Hydrogens
Smart Hydrogens
Chiral Hydrogens
Explicit Hydrogens
Abbreviate Reagents and Groups
Abbreviate Reagents
Abbreviate Groups
Do Not Abbreviate
Reaction
Plain
Equilibrium
No Go
Retro Synthetic
Resonance
Dative Bonds
Always
Metal Only
Never
Embed Title
Zoom
Rotate
Flip
